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Job Description
- Req#: JR141906
Employer Industry: Clinical Research
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Competitive benefits package focused on well-being and work-life balance
- Flexible country-specific optional benefits, including childcare vouchers and discounted gym memberships
- Chance to contribute to the advancement of innovative treatments and therapies
- Supportive and inclusive work environment
What to Expect (Job Responsibilities):
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolution of queries to maintain high-quality clinical data
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports
What is Required (Qualifications):
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills, with attention to detail
- Ability to travel at least 60% of the time, possessing a valid driver’s license
How to Stand Out (Preferred Qualifications):
- Experience working in a fast-paced clinical research environment
- Familiarity with data management systems and electronic data capture tools
- Additional certifications related to clinical research
#ClinicalResearch #HealthcareCareers #Innovation #Diversity #WorkLifeBalance
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